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Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains. [electronic resource] by
- Levavasseur, Etienne
- Laffont-Proust, Isabelle
- Morain, Emilie
- Faucheux, Baptiste A
- Privat, Nicolas
- Peoc'h, Katell
- Sazdovitch, Véronique
- Brandel, Jean-Philippe
- Hauw, Jean-Jacques
- Haïk, Stéphane
Producer: 20080924
In:
PloS one vol. 3
Availability: No items available.
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Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. [electronic resource] by
- Peoc'h, Katell
- Levavasseur, Etienne
- Delmont, Emilien
- De Simone, Alfonso
- Laffont-Proust, Isabelle
- Privat, Nicolas
- Chebaro, Yassmine
- Chapuis, Céline
- Bedoucha, Pierre
- Brandel, Jean-Philippe
- Laquerriere, Annie
- Kemeny, Jean-Louis
- Hauw, Jean-Jacques
- Borg, Michel
- Rezaei, Human
- Derreumaux, Philippe
- Laplanche, Jean-Louis
- Haïk, Stéphane
Producer: 20130515
In:
Human molecular genetics vol. 21
Availability: No items available.
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